EP0846184B1 - Solvent extraction of polyhydroxyalkanoates from biomass facilitated by the use of a marginal nonsolvent for pha - Google Patents

Solvent extraction of polyhydroxyalkanoates from biomass facilitated by the use of a marginal nonsolvent for pha Download PDF

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Publication number
EP0846184B1
EP0846184B1 EP96928198A EP96928198A EP0846184B1 EP 0846184 B1 EP0846184 B1 EP 0846184B1 EP 96928198 A EP96928198 A EP 96928198A EP 96928198 A EP96928198 A EP 96928198A EP 0846184 B1 EP0846184 B1 EP 0846184B1
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Prior art keywords
pha
polyhydroxyalkanoate
solvent
biomass
marginal
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EP96928198A
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German (de)
English (en)
French (fr)
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EP0846184A1 (en
Inventor
Isao Noda
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Procter and Gamble Co
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Procter and Gamble Co
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/62—Carboxylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/88—Post-polymerisation treatment
    • C08G63/89—Recovery of the polymer
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/62—Carboxylic acid esters
    • C12P7/625—Polyesters of hydroxy carboxylic acids

Definitions

  • the present invention relates to methods of extracting specific components from other biomass components. More specifically, the present invention relates to the extraction of a polyhydroxyalkanoate from a biological system, such as a plant or bacteria, by performing the extraction with a solvent; the extraction process being facilitated by the use of a marginal nonsolvent for PHA.
  • Commodity polymers are typically produced from petrochemical sources by well-known synthetic means.
  • bioplastic living organisms
  • PHA polyhydroxyalkanoate
  • PHA polyhydroxyalkanoate
  • Known solvent extraction methods are also limited for a large-scale separation of PHA from a biomass.
  • a commonly used solvent for the extraction of PHA from bacteria is chloroform.
  • other halogenated hydrocarbon solvents such as dichloromethane, dichlorethane and chloropropane (see, e.g., U.S. Patent 4,562,245, Stageman, issued December 31, 1985; U.S. Patent 4,324,907, Senior, Wright and Alderson, issued April 13, 1982; U.S. Patent 4,310,684, Vanlautem and Gilain, issued January 12, 1982; U.S.
  • Patent 4,705,604, Vanlautem and Gilain issued November 10, 1987; European Patent Application 036 699, Holmes and Wright, published September 3, 1981; and German Patent Application 239 609, Schmidt, Schmiechen, Rehm and Trennert, published January 10, 1986).
  • the concentrated PHA solution often forms a very high viscosity fluid or sometimes even a gel; which can be extremely difficult to process.
  • solvents are potentially harmful to health and environment if not fully removed from the PHA. Consequently, the use of a large amount of such solvents resulting in the formation of highly viscous solutions or gels, especially near the harvesting site, would be undesirable.
  • the present invention relates to a process for separating polyhydroxyalkanoate (PHA) from a biomass comprising the PHA, the process comprising: a) treating the biomass with a PHA solvent and a marginal nonsolvent for PHA; b) removing any insoluble biomass, thereby leaving behind a solution of PHA and marginal nonsolvent for PHA; and c) removing the PHA solvent from the solution, thereby resulting in a suspension of precipitated PHA in the marginal nonsolvent for PHA.
  • the process further comprises removing the marginal nonsolvent for PHA, thereby leaving behind the PHA.
  • the present invention further relates to the suspension and the PHA produced by the process.
  • Figure 1 sets forth a schematic of an embodiment of the invention wherein a marginal nonsolvent for PHA from an outside source is added (and later removed) to facilitate extraction of the PHA.
  • Alkane means a saturated hydrocarbon having the general formula C n H 2n+2 ; preferably n is from about 3 to about 20; more preferably n is from about 6 to about 16.
  • Alkenyl means a carbon-containing chain, preferably from about C 2 to about C 24 , more preferably from about C 2 to about C 19 ; which may be straight, branched or cyclic, preferably straight or branched, more preferably straight; substituted (mono- or poly-) or unsubstituted; and monounsaturated (i.e., one double or triple bond in the chain), or polyunsaturated (i.e., two or more double bonds in the chain, two or more triple bonds in the chain, or one or more double and one or more triple bonds in the chain), preferably monounsaturated.
  • Alkyl means a carbon-containing chain, preferably from about C 1 to about C 24 , more preferably from about C 1 to about C 19 ; which may be straight, branched or cyclic, preferably straight or branched, more preferably straight; substituted (mono- or poly-) or unsubstituted; and saturated.
  • Extracting polyhydroxyalkanoate from a biomass in addition to referring to the extraction of the particular PHA produced by a biomass which produces a single PHA, also refers to the extraction of one or more types of PHA when the biomass produces more than one type of PHA.
  • Polyhydroxyalkanoate and PHA mean a polymer comprising the following repeating unit: wherein R is preferably H, alkyl or alkenyl; and m is from about 1 to about 4.
  • R is preferably H, alkyl or alkenyl; and m is from about 1 to about 4.
  • the terms polyhydroxyalkanoate and PHA include polymers containing one or more different repeating units.
  • PHAs extractable by the process of the present invention preferably have a melt temperature ("Tm") of about 80°C or higher.
  • Tm melt temperature
  • such PHAs comprise at least two randomly repeating monomer units, wherein the first randomly repeating monomer unit has the structure wherein R 1 is H, or C 1 to C 2 alkyl; and n is 1 or 2; the second randomly repeating monomer unit has the structure wherein R 2 is C 3 to C 19 alkyl or C 3 to C 19 alkenyl; and wherein at least 50% of the randomly repeating monomer units have the structure of the first randomly repeating monomer unit.
  • examples of high crystallinity PHAs extractable by the present process include those disclosed in U.S. Patent Publication No.
  • WO 95/23788 Noda, filed June 6, 1995; U.S. Patent Publication No. WO 95/20614 Noda, filed April 13, 1995; U.S. Patent Publication No. WO 95/20614, Noda, filed June 5, 1995; U.S. Patent Publication No. WO 95/20614, Noda, filed June 6, 1995; U.S. Patent Publication No. WO 95/20621, Noda, filed January 28, 1994; U.S. Patent Publication No. WO 95/20621, Noda, filed June 6, 1995; U.S. Patent Publication No. WO 95/20615, Noda, filed June 7, 1995; U.S. Patent Publication No. WO 95/20615, Noda, filed June 6, 1995; and U.S. Patent 5,292,860, Shiotani and Kobayashi, issued March 8, 1994.
  • solvent means a substance capable of dissolving another substance (solute) to form a uniformly dispersed mixture (solution) at the molecular or ionic size level.
  • Nonsolvent means a substance which is incapable of appreciably dissolving another substance.
  • Marginal nonsolvent means a substance wihich is a nonsolvent by itself, however, when mixed with a solvent, becomes capable of dissolving solute.
  • Precipitant means a substance which is capable of inducing the precipitation of another substance and/or weakening the solvating power of a solvent. While a precipitant is also considered a nonsolvent, however, a nonsolvent is not always a precipitant. For example, methanol and hexane are PHA precipitants and PHA nonsolvents; whereas oil is a PHA nonsolvent, but not a very effective PHA precipitant (though at extremely high concentrations, oil will cause PHA to precipitate out of solution).
  • Sources from which PHA is extracted via the process of the present invention include single-cell organisms such as bacteria or fungi and higher organisms such as plants (herein collectively referred to as "biomass"). While such biomass could be wild-type organisms, they are preferably genetically manipulated species specifically designed for the production of a specific PHA of interest to the grower. Such genetically manipulated organisms are produced by incorporating the genetic information necessary to produce one or more types of PHA. Typically, such genetic information is derived from bacteria which naturally produce PHA.
  • Plants useful in the present invention include any genetically engineered plant designed to produce PHA.
  • Preferred plants include agricultural crops such as cereal grains, oilseeds and tuber plants; more preferably, avocado, barley, beets, broad bean, buckwheat, carrot, coconut, copra, corn (maize), cottonseed, gourd, lentils, lima bean, millet, mung bean, oat, oilpalm, peas, peanut, potato, pumpkin, rapeseed (e.g., canola), rice, sorghum, soybean, sugarbeet, sugar cane, sunflower, sweetpotato, tobacco, wheat, and yam.
  • agricultural crops such as cereal grains, oilseeds and tuber plants; more preferably, avocado, barley, beets, broad bean, buckwheat, carrot, coconut, copra, corn (maize), cottonseed, gourd, lentils, lima bean, millet, mung bean, oat, oilpalm
  • Such genetically altered fruit-bearing plants useful in the process of the present invention include, but are not limited to, apple, apricot, banana, cantaloupe, cherries, grapes, kumquat, lemon, lime, orange, papaya, peaches, pear, pineapple, tangerines, tomato, and watermelon.
  • the plants are genetically engineered to produce PHA pursuant to the methods disclosed in Poirier, Y., D.E. Dennis, K Klomparens and C. Somerville, "Polyhydroxybutyrate, a biodegradable thermoplastic, produced in transgenic plants", Science, Vol. 256, pp. 520-523 (1992); World Patent Application Publication No.
  • Particularly preferred plants are soybean, potato, corn and coconut plants genetically engineered to produce PHA; more preferably, soybean.
  • Bacteria useful in the present invention include any genetically engineered bacteria designed to produce PHA, as well as bacteria which naturally produce PHA.
  • examples of such bacteria include those disclosed in Novel Biodegradable Microbial Polymers, E.A. Dawes, ed., NATO ASI Series, Series E: Applied Sciences - Vol. 186, Kluwer Academic Publishers (1990); U.S. Patent 5,292,860, Shiotani and Kobayashi, issued March 8, 1994; U.S. Patent 5,250,430, Peoples and Sinskey, issued October 5, 1993; U.S. Patent 5,245,023, Peoples and Sinskey, issued September 14, 1993; U.S. Patent 5,229,279, Peoples and Sinskey, issued July 20, 1993.
  • the present invention relates to a process for separating polyhydroxyalkanoate (PHA) from a biomass comprising the PHA, the process comprising: a) treating the biomass with a PHA solvent and a marginal nonsolvent for PHA; b) removing any insoluble biomass, thereby leaving behind a solution of PHA and marginal nonsolvent; and c) removing the PHA solvent from the solution, thereby resulting in a suspension of precipitated PHA in the marginal nonsolvent for PHA.
  • the process further comprises removing the marginal nonsolvent for PHA, thereby leaving behind the PHA.
  • the solution formed at step b) is made up of the marginal nonsolvent for PHA dissolved or dispersed in the PHA solvent.
  • the present invention further relates to the suspension and the PHA produced by the process.
  • the PHA solvent is acetone, acetonitrile, benzene, butyl acetate, butyl propionate, ⁇ -butyrolactone, ⁇ -butyrolactone, liquified carbon dioxide, chloroform, 1,2-dichloroethane, diethyl carbonate, diethylformamide, dimethyl carbonate, dimethyl succinate, dimethyl sulfoxide, demethylformamide, 1,4-dioxane, ethyl acetate, ethylene glycol diacetate, methyl acetate, methyl ethyl ketone, 1,1,2,2-tetrachloroethane, tetrahydrofuran, 1,1,2-trichloroethane, 1,2,3-trichloropropane, toluene, xylene, or mixtures thereof.
  • the PHA solvent is acetone, acetonitrile ⁇ -butyrolactone, 1,4-dioxane, methyl acetate, toluene, methyl ethyl ketone, ethyl acetate or mixtures thereof.
  • the PHA solvent preferably is acetone, butyl acetate, ethyl acetate, methyl acetate, or mixtures thereof; more preferably acetone or ethyl acetate; more preferably still, acetone.
  • the PHA solvent is employed in the process at an elevated temperature, as the rate of dissolution of PHA in the PHA solvent at elevated temperatures has been found to be substantially faster.
  • extraction of the PHA may be conducted between about 20°C and the melt temperature of the PHA; more preferably between about 20°C and about 80°C; more preferably between about 45°C and the boiling point of the PHA solvent; more preferably still, from about 50°C to about 60°C.
  • the solid mass containing the PHA is stirred during extraction with the PHA solvent, as this also accelerates the rate of dissolution of the PHA.
  • the removal of the PHA solvent from a solution containing PHA results in the eventual precipitation of PHA as crystalline solids.
  • the concentrated PHA solution often forms a very high viscosity fluid or sometimes even a gel; which can be extremely difficult to process. If the solution contains a marginal nonsolvent for PHA which is relatively nonvolatile, the PHA will precipitate upon the removal of the PHA solvent and form a suspension in the marginal nonsolvent for PHA.
  • the present invention is exemplified in schematic form in Figure 1.
  • This process enables one to obtain the advantages of a marginal nonsolvent for PHA (e.g., oil) for the precipitating PHA, even when the marginal nonsolvent for PHA is not present in the starting biomass (e.g., non-oilseed biomass, or bacteria).
  • the marginal nonsolvent for PHA acts as a process aid by impeding the build up of excessive viscosity or gelation during the stripping of PHA solvent from the biomass.
  • the marginal nonsolvent for PHA must not significantly interfere with the solvating power of the PHA solvent, as it will be mixed with the PHA solvent during the extraction process.
  • the marginal nonsolvent for PHA should not appreciably dissolve PHA, as dissolution of the PHA would preclude suspension of the PHA as discrete particles.
  • the marginal nonsolvent for PHA is less volatile (i.e., has a lower boiling point) than the PHA solvent. Such a lower volatility will provide for easier and cleaner separation of the PHA solvent.
  • the boiling point of the marginal nonsolvent for PHA is at least about 5°C higher than the PHA solvent; more preferably at least about 10°C higher; more preferably at least about 20°C higher; more preferably still, at least about 40°C higher.
  • the marginal nonsolvent for PHA is a C 3 -C 20 alcohol, C 1 -C 20 alkane, fat, neutral lipid, oil, water, or mixtures thereof.
  • Preferred alkanes include decane, dodecane, hexadecane, and octadecane.
  • Preferred alcohols include hexanol, lauryl alcohol, octanol, oleyl alcohol, and stearyl alcohol.
  • Preferred fats include tallow, grease, and wax.
  • Preferred neutral lipids include mono-, di- and trilycerides of oleic acid, Inoleic acid and linelenic acid; lauric acid; stearic acid; and palmitic acid.
  • Preferred oils include mineral oils and vegetable oils (e.g., soybean, canola, and the like).
  • the previously described embodiments of the present invention have many surprising advantages, including avoidance of forming a high viscosity fluid or gel of PHA, which otherwise can be extremely difficult to process.
  • This is achieved by conducting the extraction of PHA in the presence of the marginal nonsolvent for PHA.
  • the marginal nonsolvent for PHA may initially serves as a miscible co-solvent to promote the extraction of PHA.
  • the marginal nonsolvent for PHA will become an effective suspending medium for the precipitating PHA (as discrete particles) due to its limited PHA-solvating power.
  • a suspension of polymer solid in a fluid nonsolvent typically has much lower apparent viscosity and thus possesses superior processability.
  • the elimination of the serious problem of gelation often encountered during the stripping of solvent from a concentrated polymer solution is an unexpected and significant advantage of the invention.
  • Another surprising advantage of the present process is its ability to produce suspensions of PHA which can be used, for example, as coatings, binders, additives for paints, food, adhesives; as well as carriers for dyes, pigments, bioactives and perfumes.
  • crystalline aliphatic polyesters like isotactic poly(3-hydroxybutyrate) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) are not appreciably soluble in ethyl acetate or acetone, even though the chemical structures of these compounds may suggest certain molecular affinity.
  • crystalline PHA containing a small amount of medium size branches can be readily dissolved in such solvents is indeed surprising.
  • Spray dried Alcaligenes eutrophus cells containing poly(3-hydoxybutyrate-co-3-hydroxyvalerate) are refluxed in methanol for 15 minutes at atmospheric pressure to remove soluble lipids.
  • the cells are dried on a tray at 30°C in an forced air tunnel. 10 g of dried cells are refluxed with a mixture of 250 mL of chloroform and 50 mL of hexadecane at atmospheric pressure for 30 minutes to extract poly(3-hydoxybutyrate-co-3-hydroxyvalerate).
  • the resultant slurries are filtered to remove cell residues.
  • the chloroform is then removed from the extraction solution under a reduced pressure, thereby leaving behind a suspension of hard solid flakes of poly(3-hydoxybutyrate-co-3-hydroxyvalerate) dispersed in hexadecane.
  • the flakes are then collected by draining hexadecane to yield 6.2 g of poly(3-hydoxybutyrate-co-3-hydroxyvalerate).
  • Psedomonas cepacia cells containing copolymer consisting mainly of 3-hydoxyoctanoate are centrifuged, decanted, and resuspended in water four times, and then freeze dried. 10 g of dried cells are refluxed with a mixture of 250 mL of acetone and 50 mL of 1-hexanol at atmospheric pressure for 20 minutes to extract the 3-hydroxyoctanoate copolymer. The resultant slurries are filtered to remove cell residues.
  • the acetone is then removed from the extraction solution under a reduced pressure, thereby leaving behind a suspension of soft solid particles of 3-hydroxyoctanoate copolymer dispersed in 1-hexanol.
  • the flakes are then collected by draining hexadecane to yield 4.8 g of copolymer.
  • transgenic potato prodeuced, e.g., by the process set forth in World Patent Application Publication No. 95/05472, Somerville, et al., published February 23, 1995; or World Patent Application Publication No. 93/02187, Somerville, et al., published February 4, 1993 sample comprising poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) containing 7.5% 3-hydroxyheptanoate repeat units is placed in a closed container charged with 600 mL of acetone and 150 mL vegetable oil and stirred for 3 hrs at 55°C. The acetone solution containing the oil and PHA is then drained from the potato using a wire-mesh filter.
  • the extraction solution containing vegetable oil, poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) and acetone is placed in a steam-heated kettle to boil off the volatile acetone, which is collected by a water-chilled condenser. After the removal of the acetone, solid flakes of poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) appear in the remaining oil which are drained by using a fine mesh filter to yield 7 g of pure vegetable oil. The polymer flakes are washed with cold acetone, previously collected by the condenser, to remove the residual entrained oil and then dried to yield 6 g of crystalline solid of poly(3-hydroxybutyrate-co-3-hydroxyheptanoate). The acetone used for the washing, is combined with the vegetable oil, and then used for further extraction of poly(3-hydroxybutyrate-co-3-hydroxyheptanoate).

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EP96928198A 1995-08-21 1996-08-16 Solvent extraction of polyhydroxyalkanoates from biomass facilitated by the use of a marginal nonsolvent for pha Expired - Lifetime EP0846184B1 (en)

Applications Claiming Priority (5)

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US2567 1993-01-11
US256795P 1995-08-21 1995-08-21
US60131796A 1996-02-16 1996-02-16
US601317 1996-02-16
PCT/US1996/013261 WO1997007229A1 (en) 1995-08-21 1996-08-16 Solvent extraction of polyhydroxyalkanoates from biomass facilitated by the use of a marginal nonsolvent for pha

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EP0846184A1 EP0846184A1 (en) 1998-06-10
EP0846184B1 true EP0846184B1 (en) 2002-05-22

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EP (1) EP0846184B1 (ko)
JP (1) JP4201834B2 (ko)
KR (1) KR100262358B1 (ko)
CN (1) CN1069345C (ko)
AT (1) ATE217908T1 (ko)
AU (1) AU704379B2 (ko)
BR (1) BR9610256A (ko)
CA (1) CA2230049C (ko)
CZ (1) CZ295187B6 (ko)
DE (1) DE69621342T2 (ko)
DK (1) DK0846184T3 (ko)
ES (1) ES2177796T3 (ko)
HK (1) HK1011871A1 (ko)
HU (1) HU222563B1 (ko)
MX (1) MX9801381A (ko)
NO (1) NO980701L (ko)
PT (1) PT846184E (ko)
RU (1) RU2196177C2 (ko)
WO (1) WO1997007229A1 (ko)

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CA2333005A1 (en) 1998-06-09 1999-12-16 Tillman U. Gerngross Methods and apparatus for the production of amorphous polymer suspensions
ATE292188T1 (de) * 1999-05-12 2005-04-15 Metabolix Inc Verfahren zur reinigung von polyhydroxyalkanoaten
JP4346441B2 (ja) 2001-11-15 2009-10-21 バイオマテラ インコーポレイテッド ゲルの調製方法
WO2004033700A1 (ja) * 2002-09-30 2004-04-22 Kaneka Corporation ポリ−３−ヒドロキシアルカン酸の凝集方法
US7491754B2 (en) 2002-11-08 2009-02-17 Kaneka Corporation Aqueous dispersion of biodegradable polyester and process for preparing the same
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JPWO2005049692A1 (ja) * 2003-11-21 2007-06-07 株式会社カネカ ポリヒドロキシアルカノエート結晶の製造方法
US7098298B2 (en) * 2003-11-21 2006-08-29 Kaneka Corporation Method for producing polyhydroxyalkanoate crystal
AU2004293501B2 (en) * 2003-11-28 2009-10-29 Phb Industrial S.A. Process for recovering polyhydroxialkanoates ("PHAs") from cellular biomass
TW200617171A (en) † 2004-06-29 2006-06-01 Procter & Gamble Improved process for the solvent-based extraction of polyhydroxyalkanoates from biomass
TW200613560A (en) 2004-06-29 2006-05-01 Procter & Gamble Solvent extraction of polyhydroxyalkanoates from biomass
ATE531748T1 (de) 2004-09-13 2011-11-15 Metabolix Inc Verfahren zur extraktion von polymeren mit einem einzigen lösungsmittel
US20060057691A1 (en) * 2004-09-15 2006-03-16 Karunakaran Narasimhan Process for the extraction of polyhydroxyalkanoates from biomass
MX2008008292A (es) * 2008-06-23 2009-12-23 Ct Investig Y Estudios Del Ipn Metodos para la produccion de polihidroxialcanoatos (pha) de cadena media usando aceite vegetal como fuente de carbono.
MY155003A (en) * 2009-01-13 2015-08-28 Plainexus Res Lab Sdn Bhd A method for producing biodegradable resins
CZ307015B6 (cs) 2014-06-03 2017-11-15 Nafigate Corporation, A.S. Způsob izolace polyhydroxyalkanoátů z biomasy fermentované mikroorganismy produkujícími polyhydroxyalkanoáty a/nebo z biomasy obsahující alespoň jednu plodinu produkující polyhydroxyalkanoáty
US20230044934A1 (en) 2019-12-23 2023-02-09 Co2Bioclean Gmbh Novel bioplastics
CN115667362A (zh) 2020-05-18 2023-01-31 文维罗科技生物技术公司 用于从富含pha的细菌生物质中分离pha的方法
EP4108776A1 (en) 2021-06-22 2022-12-28 CO2BioClean GmbH Production of biopolymers

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DE69621342D1 (de) 2002-06-27
DK0846184T3 (da) 2002-07-15
JP2000516801A (ja) 2000-12-19
RU2196177C2 (ru) 2003-01-10
AU704379B2 (en) 1999-04-22
NO980701D0 (no) 1998-02-19
CA2230049A1 (en) 1997-02-27
HU222563B1 (hu) 2003-08-28
CN1194008A (zh) 1998-09-23
HUP9901587A3 (en) 2000-06-28
ATE217908T1 (de) 2002-06-15
HK1011871A1 (en) 1999-07-23
WO1997007229A1 (en) 1997-02-27
KR100262358B1 (ko) 2000-08-01
MX9801381A (es) 1998-11-30
CZ51498A3 (cs) 1998-08-12
CA2230049C (en) 2005-11-15
DE69621342T2 (de) 2003-01-23
JP4201834B2 (ja) 2008-12-24
NO980701L (no) 1998-04-21
CZ295187B6 (cs) 2005-06-15
CN1069345C (zh) 2001-08-08
EP0846184A1 (en) 1998-06-10
ES2177796T3 (es) 2002-12-16
AU6775896A (en) 1997-03-12
PT846184E (pt) 2002-09-30
KR19990044018A (ko) 1999-06-25

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